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.beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-, 3-(trifluoromethanesulfonate) is a complex organic compound with a unique structure. It is composed of a glucoside, a propenyl group, and a trifluoromethanesulfonate group. The glucoside component is a sugar derivative with a pyranose ring structure, while the 2-propenyl and 3-trifluoromethanesulfonate groups contribute to its chemical properties and reactivity. The presence of the 1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl and phenylmethylene groups further adds to the structural complexity of .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-, 3-(trifluoromethanesulfonate). The combined features of these chemical groups likely make .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-, 3-(trifluoromethanesulfonate) useful for various applications in chemical and pharmaceutical industries.

165874-20-4

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165874-20-4 Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-, 3-(trifluoromethanesulfonate) is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs.
Used in Chemical Industry:
In the chemical industry, .beta.-D-Glucopyranoside, 2-propenyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-4,6-O-(phenylmethylene)-, 3-(trifluoromethanesulfonate) is used as a versatile reagent for the synthesis of a wide range of chemical products. Its diverse functional groups allow for various chemical reactions, making it a valuable asset in the development of new materials and compounds.
Used in Research and Development:
This complex compound is also utilized in research and development settings, where it can be employed to study the effects of different functional groups on the properties and reactivity of organic molecules. Its unique structure makes it an interesting subject for scientific investigations and may lead to the discovery of new chemical reactions and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 165874-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,8,7 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 165874-20:
(8*1)+(7*6)+(6*5)+(5*8)+(4*7)+(3*4)+(2*2)+(1*0)=164
164 % 10 = 4
So 165874-20-4 is a valid CAS Registry Number.

165874-20-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-3-O-trifluoromethanesulfonyl-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names Trifluoro-methanesulfonic acid (4aR,6R,7R,8R,8aR)-6-allyloxy-7-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:165874-20-4 SDS

165874-20-4Relevant academic research and scientific papers

Syntheses of the Fungicide/Insecticide Allosamidin and a Structural Isomer

Blattner, Regine,Furneaux, Richard H.,Kemmitt, timothy,Tyler, Peter C.,Ferrier, Robert J.,Tiden, Anna-Karin

, p. 3411 - 3422 (2007/10/02)

A synthesis of the naturally occurring inhibitor of chitin metabolism, allosamidin 1, involves, as the key step, condensation between the allosamizoline derivative 39, prepared following oxyamination of the cyclopentene 19, and the disaccharide glycosylating agent 54 which was synthesised from 2-acetamido-2-deoxy-D-glucose.The structural isomer 59 of allosamidin is also reported.Brief biological test results obtained using isomers 1 and 59 are recorded.

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